For researchers
Is your paper here?
2,657 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
51 matches for
FinnGen,
showing the first 11.
Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis
Sliz E,
Huilaja L,
Pasanen A,
Laisk T,
Reimann E,
Mägi R,
Hannula-Jouppi K,
Peltonen S,
Salmi T,
Koulu L,
Tasanen K,
Kettunen J
FinnGen · Estonian Biobank Research Team
The Journal of allergy and clinical immunology · 2022 · PMID 34454985
3 pages
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Jurgens SJ,
Rämö JT,
Kramarenko DR,
Wijdeveld LFJM,
Haas J,
Chaffin MD,
Garnier S,
Gaziano L,
Weng LC,
Lipov A,
Zheng SL,
Henry A
and 46 more — show all
Huffman JE,
Challa S,
Rühle F,
Verdugo CD,
Krijger Juárez C,
Kany S,
van Orsouw CA,
Biddinger K,
Poel E,
Elliott AL,
Wang X,
Francis C,
Ruan R,
Koyama S,
Beekman L,
Zimmerman DS,
Deleuze JF,
Villard E,
Trégouët DA,
Isnard R,
Boomsma DI,
de Geus EJC,
Tadros R,
Pinto YM,
Wilde AAM,
Hottenga JJ,
Sinisalo J,
Niiranen T,
Walsh R,
Schmidt AF,
Choi SH,
Chang KM,
Tsao PS,
Matthews PM,
Ware JS,
Lumbers RT,
van der Crabben S,
Laukkanen J,
Palotie A,
Amin AS,
Charron P,
Meder B,
Ellinor PT,
Daly M,
Aragam KG,
Bezzina CR
FinnGen · VA Million Veteran Program and 1 more consortia
Nature genetics · 2024 · PMID 39572784 · open access
3 pages
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Ollila HM,
Sharon E,
Lin L,
Sinnott-Armstrong N,
Ambati A,
Yogeshwar SM,
Hillary RP,
Jolanki O,
Faraco J,
Einen M,
Luo G,
Zhang J
and 78 more — show all
Han F,
Yan H,
Dong XS,
Li J,
Zhang J,
Hong SC,
Kim TW,
Dauvilliers Y,
Barateau L,
Lammers GJ,
Fronczek R,
Mayer G,
Santamaria J,
Arnulf I,
Knudsen-Heier S,
Bredahl MKL,
Thorsby PM,
Plazzi G,
Pizza F,
Moresco M,
Crowe C,
Van den Eeden SK,
Lecendreux M,
Bourgin P,
Kanbayashi T,
Martínez-Orozco FJ,
Peraita-Adrados R,
Benetó A,
Montplaisir J,
Desautels A,
Huang YS,
Jennum P,
Nevsimalova S,
Kemlink D,
Iranzo A,
Overeem S,
Wierzbicka A,
Geisler P,
Sonka K,
Honda M,
Högl B,
Stefani A,
Coelho FM,
Mantovani V,
Feketeova E,
Wadelius M,
Eriksson N,
Smedje H,
Hallberg P,
Hesla PE,
Rye D,
Pelin Z,
Ferini-Strambi L,
Bassetti CL,
Mathis J,
Khatami R,
Aran A,
Nampoothiri S,
Olsson T,
Kockum I,
Partinen M,
Perola M,
Kornum BR,
Rueger S,
Winkelmann J,
Miyagawa T,
Toyoda H,
Khor SS,
Shimada M,
Tokunaga K,
Rivas M,
Pritchard JK,
Risch N,
Kutalik Z,
O'Hara R,
Hallmayer J,
Ye CJ,
Mignot EJ
FinnGen
Nature communications · 2023 · PMID 37188663 · open access
2 pages
Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci
Pasanen A,
Karjalainen MK,
Zhang G,
Tiensuu H,
Haapalainen AM,
Ojaniemi M,
Feenstra B,
Jacobsson B,
Palotie A,
Laivuori H,
Muglia LJ,
Rämet M
and 1 more — show all
FinnGen
PLoS genetics · 2023 · PMID 37871108 · open access
2 pages
Risk Variants Associated With Normal Pressure Hydrocephalus: Genome-Wide Association Study in the FinnGen Cohort
Räsänen J,
Heikkinen S,
Mäklin K,
Lipponen A,
Kuulasmaa T,
Mehtonen J,
Korhonen VE,
Junkkari A,
Grenier-Boley B,
Bellenguez C,
Oinas M,
Avellan C
and 22 more — show all
Frantzén J,
Kotkansalo A,
Rinne J,
Ronkainen A,
Kauppinen M,
von Und Zu Fraunberg M,
Lönnrot K,
Satopää J,
Perola M,
Koivisto AM,
Julkunen V,
Portaankorva AM,
Mannermaa A,
Soininen H,
Helisalmi S,
Jääskeläinen JE,
Lambert JC,
Eide PK,
Palotie A,
Kurki MI,
Hiltunen M,
Leinonen V
for FinnGen
Neurology · 2024 · PMID 39141892 · open access
2 pages
High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene
Rahimov F,
Nieminen P,
Kumari P,
Juuri E,
Nikopensius T,
Paraiso K,
German J,
Karvanen A,
Kals M,
Elnahas AG,
Karjalainen J,
Kurki M
and 16 more — show all
Palotie A,
Heliövaara A,
Esko T,
Jukarainen S,
Palta P,
Ganna A,
Patni AP,
Mar D,
Bomsztyk K,
Mathieu J,
Ruohola-Baker H,
Visel A,
Fakhouri WD,
Schutte BC,
Cornell RA,
Rice DP
FinnGen · Estonian Biobank Research Team
Nature communications · 2024 · PMID 39500877 · open access
2 pages
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
Tyrmi JS,
Kaartokallio T,
Lokki AI,
Jääskeläinen T,
Kortelainen E,
Ruotsalainen S,
Karjalainen J,
Ripatti S,
Kivioja A,
Laisk T,
Kettunen J,
Pouta A
and 5 more — show all
FINNPEC Study Group, FinnGen Project, and the Estonian Biobank Research Team
JAMA cardiology · 2023 · PMID 37285119 · open access
1 page
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Burns K,
Mullin BH,
Moolhuijsen LME,
Laisk T,
Tyrmi JS,
Cui J,
Actkins KV,
Louwers YV,
Davis LK,
Dudbridge F,
Azziz R,
Goodarzi MO
and 7 more — show all
Estonian Biobank Research Team · FinnGen and 1 more consortia
BMC genomics · 2024 · PMID 38408933 · open access
1 page
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity
Rämö JT,
Kany S,
Hou CR,
Friedman SF,
Roselli C,
Nauffal V,
Koyama S,
Karjalainen J,
Maddah M,
Palotie A,
Ellinor PT,
Pirruccello JP
FinnGen
JAMA cardiology · 2024 · PMID 38477908
1 page
Genetic and functional analysis of Raynaud's syndrome implicates loci in vasculature and immunity
Tervi A,
Ramste M,
Abner E,
Cheng P,
Lane JM,
Maher M,
Valliere J,
Lammi V,
Strausz S,
Riikonen J,
Nguyen T,
Martyn GE
and 17 more — show all
Sheth MU,
Xia F,
Docampo ML,
Gu W,
Esko T,
Saxena R,
Pirinen M,
Palotie A,
Ripatti S,
Sinnott-Armstrong N,
Daly M,
Engreitz JM,
Rabinovitch M,
Heckman CA,
Quertermous T,
Jones SE,
Ollila HM
FinnGen, Estonian Biobank research team
Cell genomics · 2024 · PMID 39142284 · open access
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.